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Ratchet, swivel, tilt and roll: a complete description of subunit rotation in the ribosome
Protein synthesis by the ribosome requires large-scale rearrangements of the ‘small’ subunit (SSU; ∼1 MDa), including inter- and intra-subunit rotational motions. However, with nearly 2000 structures of ribosomes and ribosomal subunits now publicly available, it is exceedingly difficult to design ex...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881166/ https://www.ncbi.nlm.nih.gov/pubmed/36583339 http://dx.doi.org/10.1093/nar/gkac1211 |
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author | Hassan, Asem Byju, Sandra Freitas, Frederico Campos Roc, Claude Pender, Nisaa Nguyen, Kien Kimbrough, Evelyn M Mattingly, Jacob M Gonzalez Jr., Ruben L de Oliveira, Ronaldo Junio Dunham, Christine M Whitford, Paul C |
author_facet | Hassan, Asem Byju, Sandra Freitas, Frederico Campos Roc, Claude Pender, Nisaa Nguyen, Kien Kimbrough, Evelyn M Mattingly, Jacob M Gonzalez Jr., Ruben L de Oliveira, Ronaldo Junio Dunham, Christine M Whitford, Paul C |
author_sort | Hassan, Asem |
collection | PubMed |
description | Protein synthesis by the ribosome requires large-scale rearrangements of the ‘small’ subunit (SSU; ∼1 MDa), including inter- and intra-subunit rotational motions. However, with nearly 2000 structures of ribosomes and ribosomal subunits now publicly available, it is exceedingly difficult to design experiments based on analysis of all known rotation states. To overcome this, we developed an approach where the orientation of each SSU head and body is described in terms of three angular coordinates (rotation, tilt and tilt direction) and a single translation. By considering the entire RCSB PDB database, we describe 1208 fully-assembled ribosome complexes and 334 isolated small subunits, which span >50 species. This reveals aspects of subunit rearrangements that are universal, and others that are organism/domain-specific. For example, we show that tilt-like rearrangements of the SSU body (i.e. ‘rolling’) are pervasive in both prokaryotic and eukaryotic (cytosolic and mitochondrial) ribosomes. As another example, domain orientations associated with frameshifting in bacteria are similar to those found in eukaryotic ribosomes. Together, this study establishes a common foundation with which structural, simulation, single-molecule and biochemical efforts can more precisely interrogate the dynamics of this prototypical molecular machine. |
format | Online Article Text |
id | pubmed-9881166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98811662023-01-31 Ratchet, swivel, tilt and roll: a complete description of subunit rotation in the ribosome Hassan, Asem Byju, Sandra Freitas, Frederico Campos Roc, Claude Pender, Nisaa Nguyen, Kien Kimbrough, Evelyn M Mattingly, Jacob M Gonzalez Jr., Ruben L de Oliveira, Ronaldo Junio Dunham, Christine M Whitford, Paul C Nucleic Acids Res Structural Biology Protein synthesis by the ribosome requires large-scale rearrangements of the ‘small’ subunit (SSU; ∼1 MDa), including inter- and intra-subunit rotational motions. However, with nearly 2000 structures of ribosomes and ribosomal subunits now publicly available, it is exceedingly difficult to design experiments based on analysis of all known rotation states. To overcome this, we developed an approach where the orientation of each SSU head and body is described in terms of three angular coordinates (rotation, tilt and tilt direction) and a single translation. By considering the entire RCSB PDB database, we describe 1208 fully-assembled ribosome complexes and 334 isolated small subunits, which span >50 species. This reveals aspects of subunit rearrangements that are universal, and others that are organism/domain-specific. For example, we show that tilt-like rearrangements of the SSU body (i.e. ‘rolling’) are pervasive in both prokaryotic and eukaryotic (cytosolic and mitochondrial) ribosomes. As another example, domain orientations associated with frameshifting in bacteria are similar to those found in eukaryotic ribosomes. Together, this study establishes a common foundation with which structural, simulation, single-molecule and biochemical efforts can more precisely interrogate the dynamics of this prototypical molecular machine. Oxford University Press 2022-12-30 /pmc/articles/PMC9881166/ /pubmed/36583339 http://dx.doi.org/10.1093/nar/gkac1211 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Structural Biology Hassan, Asem Byju, Sandra Freitas, Frederico Campos Roc, Claude Pender, Nisaa Nguyen, Kien Kimbrough, Evelyn M Mattingly, Jacob M Gonzalez Jr., Ruben L de Oliveira, Ronaldo Junio Dunham, Christine M Whitford, Paul C Ratchet, swivel, tilt and roll: a complete description of subunit rotation in the ribosome |
title | Ratchet, swivel, tilt and roll: a complete description of subunit rotation in the ribosome |
title_full | Ratchet, swivel, tilt and roll: a complete description of subunit rotation in the ribosome |
title_fullStr | Ratchet, swivel, tilt and roll: a complete description of subunit rotation in the ribosome |
title_full_unstemmed | Ratchet, swivel, tilt and roll: a complete description of subunit rotation in the ribosome |
title_short | Ratchet, swivel, tilt and roll: a complete description of subunit rotation in the ribosome |
title_sort | ratchet, swivel, tilt and roll: a complete description of subunit rotation in the ribosome |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881166/ https://www.ncbi.nlm.nih.gov/pubmed/36583339 http://dx.doi.org/10.1093/nar/gkac1211 |
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